Union City, NJ Clinical Research Specialist Jobs - RSS Feed

Regional Clinical Research Associate

Fri, 10 Oct 2008 05:57:28 +5000

A CRO has an immediate need for an experienced Regional Clinical Research Associate.

This Regional Clinical Research Associate will be home-based and cover sites on the East Coast for a Post-Marketing Study. The initial contract is for 2 years and can be extended.

Major job duties include:
- Monitoring multiple clinical research sites.
- Follow up with sites via phone and e-mail.
- Responsible for managing regulatory site documents and binders.
- Training of site staff...

Clinical Research Scientist

Fri, 19 Sep 2008 04:54:20 +5000

Clinical Scientist

- Plan and manage clinical trial(s) including:
- Participating in the selection of investigators and study sites.
- Serve as a primary contact for the sites, responding to issues and recommending corrective actions, as well as discussing recruitment issues.
- Monitoring and tracking clinical trial progress and providing status update reports.
- Managing vendors for IVRS, central labs, IRB, etc.
- Interact and provide guidance to Field Monitors on si...

Manager, Clinical Research

Sat, 18 Oct 2008 18:23:13 +5000

Our client, a Medical Device organization located in the Northern NJ/NY area is currently seeking experienced individuals for a permanent role as a Manager of Clinical Research

JOB SUMMARY:
This individual is responsible for the overall management responsibility for IDE and post-marketing clinical trials. Manage clinical personnel and participate in budget and resource allocation to various projects. Ensure department SOPs comply with regulations and staff adheres to these SOPs. Man...

Clinical Research Associate - In-house

Fri, 31 Oct 2008 05:45:48 +5000

Our client, a pharmaceutical company located in the Northern NJ/NYC area is currently seeking qualified individuals for an In-House opportunity to work as a Clinical Research Associate. This candidate will be associated with the Virology/Infectious Disease Therapeutic area.

REQUIREMENTS
(please note, candidates lacking sufficient industry experience will not be considered)

**Bachelors Degree in Healthcare/Science/or equivalent
** 2 years of previous pharmaceutical experience...

Clinical Research Associate II

Mon, 13 Oct 2008 16:47:24 +5000

A leading pharmaceutical company is seeking a experienced Clinical Research Associate to join their dynamic team.

Responsibilities:

* Serve as a CP Study Team Leader.
* Generate (or contribute to ) study/project-related documents (protocol, regulatory documents, reports, summaries, updates for project teams and management, minutes).
* Provide CRA support to other departments and line functions e.g. GCP-QA, Drug Metabolism and Pharmacokinetics (DMPK), Drug Supply Management (D...

Clinical Research Associate II

Mon, 06 Oct 2008 21:45:37 +5000

Clinical Research Associate II

Fri, 03 Oct 2008 01:58:14 +5000

Clinical Research Associate II

Fri, 26 Sep 2008 02:41:32 +5000

Clinical Research Associate

Mon, 22 Sep 2008 23:50:03 +5000

One of our clients has an immediate opening for a CLINICAL RESEARCH ASSOCIATE in the East Coast.

The Clinical Research Associate is responsible for monitoring investigator-sponsored clinical studies, from study initiation through final monitoring (close-out) visits.

Job Duties Include:
-Managing study budgets.
-Reviewing CRF's.
-Communication with hospital IRB, NIH, and FDA.
-Writing study protocols.

Job Qualifications:
-1-2 years of experience as a CRA.
-...

Clinical Research Associate

Mon, 06 Oct 2008 22:23:45 +5000

Clinical Research Associate

Sun, 26 Oct 2008 02:40:48 +5000

PRIMARY PURPOSE OF POSITION:

The main responsibilities of the CRA include:
-Development of study specific documentation
-Monitoring and/or co-monitoring of the study
-Recruitment tracking and supervision of study sites
-Training of study personnel at investigator s sites
-Coordinating the approval process for the performance of clinical studies/notification to IRBs and authorities with regard to the respective study site
-Tracking and assurance of data quality at the s...

Bio analytical Research Associate

Fri, 10 Oct 2008 05:54:58 +5000

Bio analytical Research Associate

A well established pharmaceutical company in the Raritan New Jersey area has an immediate opening for an experienced Bio analytical Research Associate.

This individual will carry out development, validation, and implementation of analytical methods using liquid chromatography and mass spectrometry for quantification of new molecular entities in biological matrices.

Major job duties include:
*Following Good Laboratory Practices compliance<...

Clinical Scientist - Oncology

Mon, 15 Sep 2008 06:32:32 +5000

Our client, a worldwide pharmaceutical organization located in the Northern, NJ area is currently seeking qualified individuals for a contract role within their Oncology group for a Clinical Scientist.

SUMMARY:
Assists the Clinical Science Leader and clinical scientists in overall study planning, management, evaluation, and documentation. Assists or leads full protocol development and participates in study management as a clinical science representative. Provides clinical scientific i...

Clinical Trial Coordinator

Mon, 13 Oct 2008 17:26:46 +5000

A growing pharmaceutical company specializing in Cardiovascular research has an immediate need for a seasoned Clinical Trial Coordinator to join their team.

Responsibilities include:
Trial In-House Ops could also include negotiation of budget to a specified level, liaison with Legal for contract language and phone close-out visits

Set-up & maintain TMF (general, site & financial in hard copy & electronic)

Establish essential document package (includes c...

Clinical Data Manager

Sat, 18 Oct 2008 17:57:03 +5000

Our client, a fast-growing pharmaceutical company located in the Northern NJ/NYC area is currently seeking qualified candidates for a Data Management Opportunity.

QUALIFICATIONS:
Education:

Bachelor or Masters degree in life sciences (preferred), or equivalent

Experience:

Minimum 3 years of data management experience in a pharmaceutical or CRO environment (preferred)
Familiar with Electronic Data Capture (Phase Forward Inform preferred) systems
Hands o...

Clinical Supplies Planning Manager

Sat, 06 Sep 2008 06:59:42 +5000

A leading pharmaceutical company is PROACTIVELY seeking qualified candidates for a Global Clinical Supplies Project Manager position. The focus of this position is on Clinical Supplies Planning Management. This is a proactive job listing for a skill set that will open up in the future.

SUMMARY:
- Support global clinical material production activities by independently managing multiple complex projects undertaken by outside vendors.
- Drive cost effective, technically sound manufa...

Clinical Trial Assistant

Tue, 09 Sep 2008 06:52:22 +5000

The person will be the primary site contact working in conjunction with the Clinical Trial Manager, supporting Field Operations. Looking for a great personality, self-starter, take initiative, works toward process improvement.
Additional Responsibilities:
- Experience interacting with sites; making sure all documents are completed
- Working with IRB s
- Study start-up: sending out regulatory packet/binder, collecting docs, review for correctness and follow up with any questions

Sr. Regulatory Affairs Specialist

Thu, 02 Oct 2008 22:53:27 +5000

"Pharmaceutical Company located in Princeton, NJ is seeking a Sr. Regulatory Affairs Specialist to join their team"

My client is a dynamic company dedicated to the development of new pharmaceutical products for the US and global market.

Position Summary: The position is responsible for taking the lead role in IND submission preparation (IND, amendments, annual reports, etc.) and working with other regulatory affairs personnel to finalize the submission documents and ...

Clinical Administrative Assistant

Fri, 19 Sep 2008 04:21:35 +5000

"Growing Pharmaceutical Company located in Princeton, NJ is seeking a Clinical Administrative Assistant to join their team"

The role for project-related administrative support is primarily to assist the CCRM in all study-related activities as needed. All activities listed below are performed at the request of and under the direction of a CCRM. Project-related administrative support is responsible for but not limited to:

-Requesting Confidentiality Agreements for potent...

Pharmaceutical Research Scientist

Fri, 31 Oct 2008 05:58:11 +5000

A multinational biopharmaceutical company is looking for a permanent Research Scientist I/II in it's Analytical Research & Development department. Candidates will be responsible for conducting laboratory research, analytical method development and validation for formulated drug products, and routine analysis under minimal guidance of his/her supervisor. Candidates will need to possess a strong cGMP mind set and have the capability and experience to work independently with strong decision-...